Mg/Ca, Sr/Ca and Ca isotope ratios in benthonic foraminifers of surface sediment samples

We analysed Mg/Ca, Sr/Ca and Ca isotope ratios of benthonic foraminifers from sediment core tops retrieved during several research cruises in the Atlantic Ocean, in order to improve the understanding of isotope fractionation and element partitioning resulting from biomineralisation processes and changes in ambient conditions. Species include foraminifers secreting tests composed of hyaline low magnesium calcite, porcelaneous high magnesium calcite as well as aragonite. Our results demonstrate systematic isotope fractionation and element partitioning patterns specific for these foraminiferal groups. Calcium isotope fractionation is similar in porcelaneous and hyaline calcite tests and both groups demonstrate the previously described anomaly with enrichment of heavy isotopes around 3 - 4 °C (Gussone and Filipsson, 2010). Calcium isotope ratios of the aragonitic species Hoeglundina elegans, on the other hand, are about 0.4 per mil lighter compared to the calcitic species, which is in general agreement with stronger fractionation in inorganic aragonite compared to calcite. However, the low and strongly variable Sr content suggests additional processes during test formation, and we propose that transmembrane ion transport or a precursor phase to aragonite may be involved. Porcelaneous tests, composed of high Mg calcite, incorporate higher amounts of Sr compared to hyaline low Mg calcite, in agreement with inorganic calcite systematics, but also porcelaneous tests with reduced Mg/Ca show high Sr/Ca. While calcium isotopes, Sr/Ca and Mg/Ca in benthonic foraminifers primarily appear to fractionate and partition with a dominant inorganic control, d44/40Ca temperature and growth rate dependencies of benthonic foraminifer tests favour a dominant contribution of light Ca by transmembrane transport relative to unfractionated seawater Ca to the calcifying fluid, thus controlling the formation of foraminiferal d44/40Ca and Sr/Ca proxy signals.

Abundance of mesozooplankton collected in October and November 1991 at 20 stations in the South Aegean Sea during O91

The O91- Mesozooplankton dataset is based on samples collected in mid October-mid November 1991 at 20 stations in the South Aegean, the SE.Ionian Sea and in NW Levantine. Samples were collected at discrete layers (from the surface till 300m. These data are published. Sampling volume was estimated by multiplying the mouth area with the wire length. The entire sample (for deep layers) or aliquot of Taxon-specific mesozooplankton abundance (1/4) (for the upper layer) was analyzed under the binocular microscope. Copepod and cladoceran species were identified and enumerated; the other zooplankters were identified and enumerated at higher taxonomic level (commonly named as zooplankton groups). Taxonomic identification was done by I.Siokou-Frangou, E.Christou, and N.Fragopoulu, using the relevant taxonomic literature. The entire sample (for deep layers) or aliquot of Mesozooplankton total abundance (1/4) (for the upper layer) was analyzed under the binocular microscope. All zooplankters were enumerated.

Biogeography of jellyfish in the North Atlantic

In recent years a global increase in jellyfish (i.e. Cnidarians and Ctenophores) abundance and a rise in the recurrence of jellyfish outbreak events have been largely debated, but a general consensus on this matter has not been achieved yet. Within this debate, it has been generally recognised that there is a lack of reliable data that could be analysed and compared to clarify whether indeed jellyfish are increasing throughout the world ocean as a consequence of anthropogenic impact and hydroclimatic variability. Here we describe different jellyfish data sets produced within the EU program EUROBASIN, which have been assembled with the aim of presenting an up to date overview on the diversity and standing stocks of North Atlantic jellyfish. Abundance and species composition were determined in samples collected in the epipelagic layer (0- 200m), using a net well adapted to quantitatively catching gelatinous zooplankton. The samples were collected in spring-summer (April-August) 2010-2013, in inshore and offshore North Atlantic waters, between 59-68LatN and 62W-5ELong. Jellyfish were also identified and counted in samples opportunistically collected by other sampling gears in the same region and in two coastal stations in the Bay of Biscay and in the Gulf of Cadiz. Continuous Plankton Recorder (CPR) samples collected in 2009-2012 were re-analysed with the aim of identifying the time and location of jellyfish blooms across the North Atlantic basin.

Paleocene-Eocene calcareous nannofossils of onshore wells from the Coastal Plain of New Jersey and Maryland, USA

Paleogene calcareous nannofossils from split spoon cores recovered from five wells along the Coastal Plain of New Jersey and Maryland have been analyzed in order to provide onshore information complementary to that derived from the offshore DSDP Site 605 (upper continental rise off New Jersey). Hiatuses are more numerous and of greater extent in the onshore sections, but the major ones correlate well with those noted in the offshore section. At one site at least (Leggett Well), sedimentation may well have been continuous across the Cretaceous/Tertiary boundary, as it is believed to have been at DSDP Site 605. These various correlations are discussed elsewhere in a companion paper (Olsson and Wise, this volume). Important differences in nannofossil assemblages are noted between the onshore (shelf paleoenvironment) and offshore (slope-rise paleoenvironment) sections. Lithostromation simplex, not present offshore, is consistently present onshore and seems to be confined to the Eocene shelf sediments of this region. The same relationship holds for the zonal marker, Rhabdosphaera gladius Locker. The Rhomboaster-Tribrachiatus plexus is more diverse and better preserved in the onshore sections, where the lowermost Eocene Zone CP9 is well represented. Differential preservation is postulated to account for two morphotypes of Tribrachiatus bramlettei (Brönnimann and Stradner). Type A is represented at DSDP Site 605 by individuals with short, stubby arms, but these forms are not present in the equivalent onshore sections. There they are replaced by the Type B morphotypes, which exhibit a similar basic construction but possess much longer, more delicate arms.

Paleogene calcareous nannofossil biostratigraphy of DSDP Hole 21-210

The major objectives of Leg 133 were (1) to define the evolution of the carbonate platforms on the northeastern Australian margin, including their relationship to adjoining basins; and (2) to understand the effects of climate and sea level on their development in space and time (Davies, McKenzie, Palmer-Julson, et al., 1991, doi:10.2973/odp.proc.ir.133.1991). Sixteen sites were drilled, and more than 5.5 km of Neogene core was recovered during Leg 133. However, recovery of Paleogene sediments was unexpectedly poor (a total of a few meters), and the sediments were poorly dated because of strong diagenesis. On the other hand, Site 210 drilled in this region during Leg 21 yielded an expanded Paleogene section, which contains abundant calcareous microfossils. Biostratigraphic information for this section given in Burns, Andrews, et al. (1973, doi:10.2973/dsdp.proc.21.1973) was based primarily on shipboard results. Detailed calcareous nannofossil and planktonic foraminifer biostratigraphies have not been published. Here we provide a detailed documentation of the calcareous nannofossil distribution in the section, biostratigraphically date the section using the modern nannofossil zonation of Okada and Bukry (1980. doi:10.1016/0377-8398(80)90016-X), and construct an age-depth curve based on current knowledge of nannofossil magnetobiochronology. This should provide a useful Paleogene biostratigraphic reference in the northeastern Australian sea, as Site 210 has apparently yielded the most complete Paleogene record in the region. The detailed biostratigraphy should provide a better age constraint for the regional Eocene-Oligocene hiatus recognized previously (e.g., Jenkins and Srinivasan, 1986, doi:10.2973/dsdp.proc.90.113.1986) and should be useful for future studies on various aspects of Paleogene history of the northeastern Australian sea.

Planktonic foraminifera stratigraphy of ODP Holes 198-1209C and 198-1211C

During Leg 198, the Cretaceous/Paleocene (K/P) boundary was recovered in a remarkable set of cores in nine separate holes at Sites 1209, 1210, 1211, and 1212 on the Southern High of Shatsky Rise. The boundary succession includes an uppermost Maastrichtian white to very pale orange, slightly indurated nannofossil ooze overlain by lowermost Paleocene grayish orange foraminiferal ooze. The boundary between the uppermost Maastrichtian and the lowermost Paleocene is clearly bioturbated. The contact surface is irregular, and pale orange burrows extend 10 cm into the white Maastrichtian ooze. Preliminary investigations conducted on board revealed that the deepest sections of these burrows yielded highly abundant, minute planktonic foraminiferal assemblages dominated by Guembelitria with rare Hedbergella holmdelensis and Hedbergella monmouthensis, possibly attributable to the lowermost Paleocene Zone P0. The substantial thickness of the uppermost Maastrichtian Micula prinsii (CC26) nannofossil Zone and the lowermost Danian Parvularugoglobigerina eugubina (Palpha) foraminiferal Zone suggested that the K/P boundary was rather expanded compared to the majority of deep-sea sites (see Bralower, Premoli Silva, Malone, et al., 2002, doi:10.2973/odp.proc.ir.198.2002). This data report concerns the planktonic foraminiferal biostratigraphy across the K/P boundary in Hole 1209C, the shallowest site (2387 m water depth), and in Hole 1211C, the deepest site (2907 m water depth), where the foraminiferal record across the boundary appeared to be best preserved.

Ice and chlorophyll a concentration and mesozooplankton characteristics during two 'On Thin Ice' cruises, northern Svalbard waters

The spatial variation in mesozooplankton biomass, abundance and species composition in relation to oceanography was studied in different climatic regimes (warm Atlantic vs. cold Arctic) in northern Svalbard waters. Relationships between the zooplankton community and various environmental factors (salinity, temperature, sampling depth, bottom depth, sea-ice concentrations, algal biomass and bloom stage) were established using multivariate statistics. Our study demonstrated that variability in the physical environment around Svalbard had measurable effect on the pelagic ecosystem. Differences in bottom depth and temperature-salinity best explained more than 40% of the horizontal variability in mesozooplankton biomass (DM/m**2) after adjusting for seasonal variability. Salinity and temperature also explained much (21% and 15%, respectively) of the variability in mesozooplankton vertical distribution (ind./m**3) in August. Algal bloom stage, chlorophyll-a biomass, and depth stratum accounted for additional 17% of the overall variability structuring vertical zooplankton distribution. Three main zooplankton communities were identified, including Atlantic species Fritillaria borealis, Oithona atlantica, Calanus finmarchicus, Themisto abyssorum and Aglantha digitale; Arctic species Calanus glacialis, Gammarus wilkitzkii, Mertensia ovum and Sagitta elegans; and deeper-water inhabitants Paraeuchaeta spp., Spinocalanus spp., Aetideopsis minor, Mormonilla minor, Scolecithricella minor, Gaetanus (Gaidius) tenuispinus, Ostracoda, Scaphocalanus brevicornis and Triconia borealis. Zooplankton biomasses in Atlantic- and Arctic-dominated water masses were similar, but biological ''hot-spots'' were associated with Arctic communities.